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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02941952 |
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Date of registration:
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20/10/2016 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Comparative Noninvasive Continuous Cardiac Output by the Clearsight® With Invasive Monitoring by PICCO® in Abdominal Major Surgery
CLEARPICCO |
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Scientific title:
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Date of first enrolment:
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October 28, 2016 |
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Target sample size:
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02941952 |
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Study type:
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Interventional |
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Study design:
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Phase:
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N/A
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Countries of recruitment
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France
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients scheduled to undergo major abdominal surgery
- Patients monitored by a PICCO® device
Exclusion Criteria:
- Patients with heart rhythm disorder
- Patients with Raynaud's disease or vasculitis
- Emergency surgery
- Significant edema fingers
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Cardiac Output Measurement
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Intervention(s)
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Device: Cardiac output and stroke ejection volume monitoring with both ClearSight® and PICCO® in major abdominal surgery.
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Primary Outcome(s)
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Stroke ejection volume (SEV) measure by ClearSight®
[Time Frame: 24 hours]
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Stroke ejection volume measure by PICCO®
[Time Frame: 24 hours]
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Secondary ID(s)
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2016-A01283-48
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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